A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17393809



Internal ID22451679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206995977..207004088hg38UCSC Ensembl
chr2:207860701..207868812hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg388112
hg198112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898524
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17393809
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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